The Development Regulatory Affairs for Oncology Medicinal Products 2015 is a webinar that covers topics such as:
Regulatory strategy in oncology
Covered in the Session:
Small patients populations
One pivotal study
Faster approval pathways
Scientific advice
The Development Regulatory Affairs for Oncology Medicinal Products 2015 is intended for:
Project Managers
Senior management
CRAs and CRCs
Medical writers
Investigators
QA / Compliance personnel
QA / QC Auditors and Staff
Clinical Research Scientists
Consultants
Past Events
Development Regulatory Affairs for Oncology Medicinal Products 2015 - 30 Jun 2015, Webinar (52088)
Important
Please, check "Development Regulatory Affairs for Oncology Medicinal Products" official website for possible changes, before making any traveling arrangements
Event Categories
Education: Training
Health & Medicine: Medical laboratories, Medical technology
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